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Items: 1 to 20 of 358

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148184copy number variation1nstd102humanPathogenic GRCh38 chr1: 243,221,458-248,919,110 , GRCh37.p13 chr1: 243,384,760-249,213,309 LOC105373271, LOC107985725, 153 more genes
    nsv7099272copy number variation1nstd231human GRCh38.p12 chr1: 243,197,153-248,437,482 , GRCh37 chr1: 243,360,455-248,600,783 ADSS2, HNRNPU, 124 more genes
    nsv7098854copy number variation1nstd102humanPathogenic GRCh37 chr1: 245,704,069-249,212,562 , GRCh38.p12 chr1: 245,540,767-248,918,363 OR2X1P, OR14A2, 118 more genes
    nsv7055426inversion1nstd229human GRCh38 chr1: 247,429,281-247,845,194 , GRCh37.p13 chr1: 247,592,583-248,008,496 OR14L1, OR6R1P, 19 more genes
    nsv7049735inversion1nstd229human GRCh38 chr1: 247,664,727-247,954,522 , GRCh37.p13 chr1: 247,828,029-248,117,824 OR2T8, OR6F1, 17 more genes
    nsv7049548inversion1nstd229human GRCh38 chr1: 247,434,792-247,854,366 , GRCh37.p13 chr1: 247,598,094-248,017,668 OR2G2, LOC102724446, 19 more genes
    nsv7041671inversion1nstd229human GRCh38 chr1: 247,239,306-248,299,501 , GRCh37.p13 chr1: 247,402,608-248,462,803 OR9H1P, OR2L9P, 49 more genes
    nsv6678082copy number variation1nstd229human GRCh38 chr1: 247,782,599-247,945,122 , GRCh37.p13 chr1: 247,945,901-248,108,424 OR2X1P, OR2W3, 9 more genes
    nsv6676591copy number variation1nstd229human GRCh38 chr1: 247,742,306-248,679,100 , GRCh37.p13 chr1: 247,905,608-248,842,401 OR14A2, OR2T29, 50 more genes
    nsv6675868copy number variation1nstd229human GRCh38 chr1: 247,840,153-248,617,375 , GRCh37.p13 chr1: 248,003,455-248,780,676 CLK3P2, OR2T7, 41 more genes
    nsv6675088copy number variation1nstd229human GRCh38 chr1: 247,776,046-247,851,138 , GRCh37.p13 chr1: 247,939,348-248,014,440 OR6R1P, OR11L1, 3 more genes
    nsv6673925copy number variation1nstd229human GRCh38 chr1: 247,506,357-247,841,446 , GRCh37.p13 chr1: 247,669,659-248,004,748 OR14A2, OR14L1, 16 more genes
    nsv6667957copy number variation1nstd229human GRCh38 chr1: 247,515,980-247,913,359 , GRCh37.p13 chr1: 247,679,282-248,076,661 OR2C3, OR6F1, 18 more genes
    nsv6665900copy number variation1nstd229human GRCh38 chr1: 247,656,440-248,785,565 , GRCh37.p13 chr1: 247,819,742-248,865,778 OR2X1P, OR3D1P, 60 more genes
    nsv6659533copy number variation1nstd229human GRCh38 chr1: 247,373,080-248,325,181 , GRCh37.p13 chr1: 247,536,382-248,488,483 OR2L3, OR2L5, 47 more genes
    nsv6659249copy number variation1nstd229human GRCh38 chr1: 247,556,814-248,422,746 , GRCh37.p13 chr1: 247,720,116-248,586,047 OR2L13, TRIM58, 44 more genes
    nsv6637024copy number variation1nstd102humanUncertain significance GRCh37 chr1: 247,588,318-248,022,379 , GRCh38.p12 chr1: 247,425,016-247,859,077 OR14L1, OR11L1, 20 more genes
    nsv6636794copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,972,939-249,224,684 , GRCh38.p12 chr1: 223,785,237-248,930,485 SEPTIN7P13, WNT3A, 546 more genes
    nsv6636648copy number variation1nstd102humanPathogenic GRCh37 chr1: 239,910,960-249,224,684 , GRCh38.p12 chr1: 239,747,660-248,930,485 RFKP1, OR2T29, 206 more genes
    nsv6636282copy number variation1nstd102humanPathogenic GRCh37 chr1: 243,258,050-249,224,684 , GRCh38.p12 chr1: 243,094,748-248,930,485 AHCYP8, OR2M2, 154 more genes
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